Rodent models of glaucoma and their applicability for drug discovery

被引:37
作者
Agarwal, Renu [1 ]
Agarwal, Puneet [2 ]
机构
[1] Univ Teknologi MARA, Fac Med, Ctr Res Neurosci, Sungai Buloh Campus, Shah Alam, Selangor, Malaysia
[2] Int Med Univ, Fac Med, IMU Clin Campus, Seremban, Malaysia
关键词
Glaucoma models; rodents; intraocular pressure; retinal ganglion cells; optic nerve; OPTIC-NERVE TRANSECTION; GANGLION-CELL DEATH; INDUCED OCULAR HYPERTENSION; POSTERIOR SEGMENT CHANGES; INTRAOCULAR-PRESSURE; RAT MODEL; RETINAL ISCHEMIA; ADULT ALBINO; MAGNESIUM ACETYLTAURATE; TRABECULAR MESHWORK;
D O I
10.1080/17460441.2017.1281244
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Rodents have widely been used to represent glaucomatous changes both in the presence and absence of elevated intraocular pressure (IOP) as they offer clear advantages over other animal species. IOP elevation is commonly achieved by creating an obstruction in the aqueous outflow pathways, consequently leading to retinal ganglion cell and optic nerve (ON) damage, the hallmark of glaucoma. These changes may also be achieved in the absence of elevated IOP by directly inflicting injury to retina or ON. Areas covered: This paper presents a summary of currently used rodent models of glaucoma. The characteristics of these models from several studies are summarized. The benefits and shortcomings of these models are also discussed. Expert opinion: The choice of animal model that closely represents human disease is key for successful translational of preclinical research to clinical practice. Rodent models of rapid IOP elevation are likely to be least representative, whereas models such as steroid-induced glaucoma models more closely resemble the trabecular meshwork changes seen in glaucomatous human eyes. However, this model needs further characterization. Rodent models based on direct retinal and ON injury are also useful tools to investigate molecular mechanisms involved at the site of final common pathology and neuroprotective strategies.
引用
收藏
页码:261 / 270
页数:10
相关论文
共 99 条
[1]  
Agarwal R, 2016, EXP BIOL MED MAYWOOD
[2]   Current concepts in the pathophysiology of glaucoma [J].
Agarwal, Renu ;
Gupta, Suresh K. ;
Agarwal, Puneet ;
Saxena, Rohit ;
Agrawal, Shyam S. .
INDIAN JOURNAL OF OPHTHALMOLOGY, 2009, 57 (04) :257-266
[3]   Experimental mouse ocular hypertension: Establishment of the model [J].
Aihara, M ;
Lindsey, JD ;
Weinreb, RN .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (10) :4314-4320
[4]   Ocular hypertension in mice with a targeted type I collagen mutation [J].
Aihara, M ;
Lindsey, JD ;
Weinreb, RN .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (04) :1581-1585
[5]  
Alarcón-Martínez L, 2009, MOL VIS, V15, P2373
[6]   Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice [J].
Anderson, MG ;
Smith, RS ;
Hawes, NL ;
Zabaleta, A ;
Chang, B ;
Wiggs, JL ;
John, SWM .
NATURE GENETICS, 2002, 30 (01) :81-85
[7]   Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice [J].
Anderson, Michael G. ;
Smith, Richard S. ;
Savinova, Olga V. ;
Hawes, Norman L. ;
Chang, Bo ;
Zabaleta, Adriana ;
Wilpan, Robert ;
Heckenlively, John R. ;
Davisson, Muriel ;
John, Simon W. M. .
BMC GENETICS, 2001, 2 (1)
[8]   PROTECTIVE EFFECT OF MAGNESIUM ACETYLTAURATE AGAINST ENDOTHELIN-INDUCED RETINAL AND OPTIC NERVE INJURY [J].
Arfuzir, N. N. N. ;
Lambuk, L. ;
Jafri, A. J. A. ;
Agarwal, R. ;
Iezhitsa, I. ;
Sidek, S. ;
Agarwal, P. ;
Bakar, N. S. ;
Kutty, M. K. ;
Yusof, A. P. Md ;
Krasilnikova, A. ;
Spasov, A. ;
Ozerov, A. ;
Ismail, N. Mohd .
NEUROSCIENCE, 2016, 325 :153-164
[9]   Glutamate transporter localization does not correspond to the temporary functional recovery and late degeneration after acute ocular ischemia in rats [J].
Barnett, NL ;
Grozdanic, SD .
EXPERIMENTAL EYE RESEARCH, 2004, 79 (04) :513-524
[10]  
Bayer AU, 2001, INVEST OPHTH VIS SCI, V42, P1258